Investigating the Effects of Altering Portion Size Reduction Awareness on Compensatory Eating Behaviour

Sponsor
University of Liverpool (Other)
Overall Status
Recruiting
CT.gov ID
NCT06119295
Collaborator
(none)
108
1
3
6
18

Study Details

Study Description

Brief Summary

The present study aims to investigate whether energy intake is reduced when participants consume a reduced portion size (15% compared to the 'control' portion), and also to see whether awareness of this reduction affects energy intake.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Portion size manipulation
N/A

Detailed Description

In the present study, all participants will participate in two sessions - the baseline session and the experimental session. In the baseline session, participants will be given ad libitum access to a lunch meal (followed by ad libitum access to dessert), and ad libitum access to a dinner meal (followed by ad libitum access to dessert). Then, after a washout period of between 1-6 weeks, participants will return to complete the experimental session, where they will be randomised to one of three conditions:

Condition 1 (control condition): The same as the baseline condition except that the lunch will be of a fixed portion which participants must consume all of - this portion size will be the same amount of food as was consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served is the same as the amount they consumed in the baseline session).

Condition 2 (reduced aware condition): The same as the baseline condition except that the lunch will be of a fixed portion which participants must consume all of - this portion size will be 15% less than the amount of food consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served has been reduced from the amount they consumed in the baseline session).

Condition 3 (reduced unaware condition): The same as the baseline condition except that the lunch will be of a fixed portion which participants must consume all of - this portion size will be 15% less than the amount of food consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served is the same as the amount they consumed in the baseline session).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
108 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Investigating the Effects of Altering Portion Size Reduction Awareness on Compensatory Eating Behaviour
Anticipated Study Start Date :
Oct 30, 2023
Anticipated Primary Completion Date :
Apr 30, 2024
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Control Condition

Participants will be served a lunch - this will be of a fixed portion - this portion size will be the same amount of food as was consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served is the same as the amount they consumed in the baseline session).

Behavioral: Portion size manipulation
The intervention will be administered via changing portion sizes of foods served to participants. Depending on the condition participants are in, they will be served either a portion size which consists of the amount of food they consumed in the first test session, or a reduced portion size. Within these two reduced portion size conditions, one group of participants will be made aware that their portion size has been reduced, the other will not and instead will be told that this portion size is the same as the amount of food they consumed in the previous session.

Experimental: Reduce aware condition

Participants will be served a lunch - this will be of a fixed portion - this portion size will be 15% less than the amount of food consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served has been reduced from the amount they consumed in the baseline session).

Behavioral: Portion size manipulation
The intervention will be administered via changing portion sizes of foods served to participants. Depending on the condition participants are in, they will be served either a portion size which consists of the amount of food they consumed in the first test session, or a reduced portion size. Within these two reduced portion size conditions, one group of participants will be made aware that their portion size has been reduced, the other will not and instead will be told that this portion size is the same as the amount of food they consumed in the previous session.

Experimental: Reduced unaware condition

Participants will be served a lunch - this will be of a fixed portion - this portion size will be 15% less than the amount of food consumed in the ad libitum lunch meal in the baseline session (participants will be told that the amount of food served is the same as the amount they consumed in the baseline session).

Behavioral: Portion size manipulation
The intervention will be administered via changing portion sizes of foods served to participants. Depending on the condition participants are in, they will be served either a portion size which consists of the amount of food they consumed in the first test session, or a reduced portion size. Within these two reduced portion size conditions, one group of participants will be made aware that their portion size has been reduced, the other will not and instead will be told that this portion size is the same as the amount of food they consumed in the previous session.

Outcome Measures

Primary Outcome Measures

  1. Immediate energy intake post-fixed lunch meal [Within 30 minutes after intervention administered]

    Amount of energy consumed from the lunch dessert

  2. Total delayed post-fixed lunch meal energy intake [Within 10 hours after intervention administered]

    Amount of energy consumed from the post-lunch snack box intake, dinner meal, dinner dessert, post-dinner snack box intake, additional energy intake

  3. Total post-fixed lunch meal energy intake [Within 10 hours after intervention administered]

    Amount of energy consumed from the lunch dessert, post-lunch snack box intake, dinner meal, dinner dessert, post-dinner snack box intake, additional energy intake

Secondary Outcome Measures

  1. Post-lunch snack box intake [Within 4 hours after intervention administered]

    Amount of energy consumed from snack box consumed between lunch and dinner

  2. Total intake of the ad libitum dinner meal [Within 4-5 hours after intervention administered]

    Amount of energy consumed from the dinner meal

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • United Kingdom (UK) residents able to visit laboratory on campus in Liverpool, aged ≥ 18

  • Body Mass Index (BMI) between 18.5 and 32.5 kg/m2

  • Proficiency in English language

  • Self-report willingness to eat each of the test foods

Exclusion Criteria:
  • Current medication use which affects appetite

  • Pregnant

  • Currently or previously diagnosed with an eating disorder

  • Currently on a diet

  • Have any food allergies or intolerances

  • Are vegan

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Liverpool Liverpool United Kingdom L69 7ZA

Sponsors and Collaborators

  • University of Liverpool

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Liverpool
ClinicalTrials.gov Identifier:
NCT06119295
Other Study ID Numbers:
  • Portion size reduction study
First Posted:
Nov 7, 2023
Last Update Posted:
Nov 9, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 9, 2023